A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092417



Internal ID22001650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67849297..67849297hg38UCSC Ensembl
chr10:69609055..69609055hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092417
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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